Sr Validation Specialist

• →Execute commissioning and qualification activities for packaging equipment and systems within PD environments.
• →Support the development and execution of C&Q documentation, including protocols, test scripts, and reports.
• →Collaborate with cross-functional teams such as Engineering, Quality, Manufacturing, and PD to ensure alignment and project success.
• →Assist in troubleshooting and resolving issues related to packaging systems during qualification activities.
• →Ensure compliance with cGMP and internal quality standards.
• →Maintain accurate documentation and provide timely updates on project progress.
• →Support continuous improvement initiatives within packaging and qualification processes.

• Mid-level experience in Commissioning & Qualification within pharmaceutical, biotechnology, or medical device industries.
• Experience or exposure to packaging equipment and processes is preferred.
• Strong sense of ownership, accountability, and initiative.
• Ability to work independently and manage priorities in a dynamic environment.
• Strong communication and problem-solving skills.

• Availability to work 2nd and 3rd shifts as required to support project timelines.

• Familiarity with cGMP regulations and validation lifecycle.
• Experience working in Process Development (PD) environments is a plus.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.